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TRIETHYL 2-PHOSPHONOPROPIONATE

Basic information Safety Supplier Related

TRIETHYL 2-PHOSPHONOPROPIONATE Basic information

Product Name:
TRIETHYL 2-PHOSPHONOPROPIONATE
Synonyms:
  • TRIETHYL 2-PHOSPHONOPROPIONATE
  • 2-DIETHYLPHOSPHONOPROPIONIC ACID ETHYL ESTER
  • DIETHYL ETHOXYCARBONYLETHYL-PHOSPHONATE
  • ETHYL-2-(DIETHYLPHOSPHONO)PROPANOATE
  • Diethyl 1-(ethoxycarbonyl)ethanephosphonate~2-Phosphonopropionic acid triethyl ester
  • Triethyl2-phosphonopropionate,98%
  • 2-phosphonopropionic acid triethyl ester
  • diethyl 1-(ethoxycarbonyl)ethanephosphonate
CAS:
3699-66-9
MF:
C9H19O5P
MW:
238.22
EINECS:
223-033-4
Product Categories:
  • LJ
  • Small molecule
  • C-C Bond Formation
  • Horner-Wadsworth-Emmons Reagents
  • Olefination
Mol File:
3699-66-9.mol
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TRIETHYL 2-PHOSPHONOPROPIONATE Chemical Properties

Melting point:
161-164°
Boiling point:
143-144 °C12 mm Hg(lit.)
Density 
1.111 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.431(lit.)
Flash point:
192 °F
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Miscible with chloroform and methanol.
form 
Liquid
color 
Clear colorless
Specific Gravity
1.111
BRN 
1786994
InChIKey
BVSRWCMAJISCTD-UHFFFAOYSA-N
CAS DataBase Reference
3699-66-9(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38-38-37-36
Safety Statements 
23-24/25-36-26-39-37
RIDADR 
1993
WGK Germany 
3
10
Hazard Note 
Irritant
HS Code 
29319019

MSDS

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TRIETHYL 2-PHOSPHONOPROPIONATE Usage And Synthesis

Chemical Properties

CLEAR COLOURLESS LIQUID

Uses

Triethyl 2-Phosphonopropionate is used in studies involving insecticides and their efficacy on various bacterium. Also act as inhibitors of Epstein-Bar virus transmission and infections.

Uses

Triethyl 2-phosphonopropionate is used as a reactant in intramolecular conjugate addition for the synthesis of floresolide B, enantioselective synthesis of spiroindane di-methyl acetic acid and in stereo selective intramolecular Diels-Alder reactions. It plays an important role in Horner-Wadsworth-Emmons reactions and chemoenzymatic one-pot synthesis of gamma-butyrolactones. It is also used in the preparation of 3-[2]furyl-2-methyl-acrylic acid ethyl ester by reacting with furfural.

Purification Methods

Purify it by fractional distillation with high reflux ratio, preferably using a spinning band column. [Kosolapoff & Powell J Am Chem Soc 72 4198 1950, Kresze et al. Justus Liebigs Ann Chem 756 112 1972, Beilstein 4 IV 3617.]

TRIETHYL 2-PHOSPHONOPROPIONATESupplier

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